DCR LABS HAND SANITIZER- ethyl alcohol gel

DCR Labs Hand Sanitizer by

Drug Labeling and Warnings

DCR Labs Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62%

PURPOSE

Antiseptic

INDICATIONS & USAGE

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

WARNINGS

For external use only. Flammable-keep away from fire or flame. When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water, avoid contact with broken skin, and do not inhale or ingest. Stop use and ask a doctor if rash or irritation develops and lasts for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

INACTIVE INGREDIENT

Water, Isopropyl Alcohol, Tocopheryl Acetate, Glycerin, Propylene Glycol, Isopropyl Myristate, Carbomer, Aminomethyl Propanol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DCR LABS HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72839-157
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CARBOMER 940 (UNII: 4Q93RCW27E)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72839-157-08	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/26/2020
2	NDC: 72839-157-16	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/26/2020

Labeler - Derma Care Research Labs, LLC (116817470)

Registrant - Derma Care Research Labs, LLC (116817470)